Primary Pigmented Nodular Adrenocortical Disease (PPNAD)

Alias:
Pigmented Nodular Adrenocortical Disease, Primary, 2
Pigmented Nodular Adrenocortical Disease, Primary, 1
Primary Pigmented Nodular Adrenal Dysplasia
Ppnad
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Primary Pigmented Nodular Adrenocortical Disease, also known as pigmented nodular adrenocortical disease, primary, 2, is related to pigmented nodular adrenocortical disease, primary, 1 and pituitary-dependent cushing's disease. An important gene associated with Primary Pigmented Nodular Adrenocortical Disease is PRKAR1A (Protein Kinase CAMP-Dependent Type I Regulatory Subunit Alpha), and among its related pathways/superpathways are Infectious disease and Signal Transduction. The drugs Racepinephrine and Adrenocorticotropic Hormone have been mentioned in the context of this disorder. Affiliated tissues include adrenal cortex and cortex, and related phenotypes are Decreased viability and Decreased substrate adherent cell growth
Related ID:
MESH:C566469

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
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16
110
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Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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IF
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